Canonical Allele Identifier: CA2736050756

Gene: MED25

Linked Data

• dbSNP Id: rs2123878616

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49829954_49829955insGTGGCTCAGCC , CM000681.2:g.49829954_49829955insGTGGCTCAGCC	GRCh38
NC_000019.9:g.50333211_50333212insGTGGCTCAGCC , CM000681.1:g.50333211_50333212insGTGGCTCAGCC	GRCh37
NC_000019.8:g.55025023_55025024insGTGGCTCAGCC	NCBI36
NG_017091.1:g.16676_16677insGTGGCTCAGCC , LRG_368:g.16676_16677insGTGGCTCAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.688+6_688+7insGTGGCTCAGCC	ENSP00000470692.3:n.688+6_688+7insGTGGCTCAGCC
ENST00000312865.10:c.688+6_688+7insGTGGCTCAGCC MANE Select	ENSP00000326767.5:n.688+6_688+7insGTGGCTCAGCC
ENST00000538643.5:c.181-557_181-556insGTGGCTCAGCC	ENSP00000437496.1:n.181-557_181-556insGTGGCTCAGCC
ENST00000595185.5:c.688+6_688+7insGTGGCTCAGCC	ENSP00000470027.1:n.688+6_688+7insGTGGCTCAGCC
ENST00000612791.4:c.686+6_686+7insGTGGCTCAGCC	ENSP00000479851.1:n.686+6_686+7insGTGGCTCAGCC
ENST00000612854.4:c.450+939_450+940insGTGGCTCAGCC	ENSP00000482155.1:n.450+939_450+940insGTGGCTCAGCC
ENST00000617849.4:c.158-785_158-784insGTGGCTCAGCC	ENSP00000484882.1:n.158-785_158-784insGTGGCTCAGCC
ENST00000618715.4:c.158-784_158-783insGTGGCTCAGCC	ENSP00000480731.1:n.158-784_158-783insGTGGCTCAGCC
ENST00000620467.4:c.688+6_688+7insGTGGCTCAGCC	ENSP00000482659.1:n.688+6_688+7insGTGGCTCAGCC
ENST00000622402.4:c.146-5873_146-5872insGTGGCTCAGCC	ENSP00000478074.1:n.146-5873_146-5872insGTGGCTCAGCC
NM_030973.3:c.688+6_688+7insGTGGCTCAGCC , LRG_368t1:c.688+6_688+7insGTGGCTCAGCC	NP_112235.2:n.688+6_688+7insGTGGCTCAGCC
XM_011527353.1:c.688+6_688+7insGTGGCTCAGCC	XP_011525655.1:n.688+6_688+7insGTGGCTCAGCC
NM_001378355.1:c.688+6_688+7insGTGGCTCAGCC	NP_001365284.1:n.688+6_688+7insGTGGCTCAGCC
NM_030973.4:c.688+6_688+7insGTGGCTCAGCC MANE Select	NP_112235.2:n.688+6_688+7insGTGGCTCAGCC